ClinVar Miner

List of variants reported as benign for Rett syndrome

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Total variants: 18
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NM_001110792.2(MECP2):c.1134_1136CCA[1] (p.His383_His384del) rs61752381
NM_001110792.2(MECP2):c.1225G>A (p.Glu409Lys) rs56268439
NM_001110792.2(MECP2):c.1269C>T (p.Ser423=) rs3027928
NM_001110792.2(MECP2):c.1366G>A (p.Ala456Thr) rs61753975
NM_001110792.2(MECP2):c.623C>G (p.Thr208Ser) rs61749713
NM_001110792.2(MECP2):c.626C>T (p.Thr209Met) rs61749714
NM_001110792.2(MECP2):c.813C>T (p.Ala271=) rs1042870
NM_004992.3(MECP2):c.1072G>A (p.Ala358Thr) rs147017239
NM_004992.3(MECP2):c.1126C>T (p.Pro376Ser) rs61752387
NM_004992.3(MECP2):c.1129_1198del (p.Lys377fs) rs1557135353
NM_004992.3(MECP2):c.1161C>T (p.Pro387=) rs61750246
NM_004992.3(MECP2):c.1162C>G (p.Pro388Ala) rs61753000
NM_004992.3(MECP2):c.1180G>A (p.Glu394Lys) rs63094662
NM_004992.3(MECP2):c.377+28A>G rs185036026
NM_004992.3(MECP2):c.378-17del rs61753982
NM_004992.3(MECP2):c.378-20C>G rs368684221
NM_004992.3(MECP2):c.819G>T (p.Gly273=) rs61750245

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